6 results
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29ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
×
BeneVision N12, BeneVision N15, BeneVision N17, BeneVision N19, BeneVision N22, BeneVision N1
FDA 510(k)
FDA Class 2
·Cardiovascular
MODIFICATION TO PROMAX-XP, TENS AND MICROCURRENT DEVICE; PROMAX-TENS, TENS DEVICE; PROMAX-LIBRA, TENS DEVICE; PROMAX-MIC
FDA 510(k)
FDA Class 2
·Neurology
SPINAL EPIDURAL NEEDLES
FDA 510(k)
FDA Class 2
·Anesthesiology
Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
FDA classification
FDA Class 2
·Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Needle, Conduction, Anesthetic (W/Wo Introducer)
FDA classification
FDA Class 2
·Needle, Conduction, Anesthetic (W/Wo Introducer)
Stimulator, Nerve, Transcutaneous, For Pain Relief
FDA classification
FDA Class 2
·Stimulator, Nerve, Transcutaneous, For Pain Relief